Annual or perennial, terrestrial, amphibious or aquatic herbs, sometimes undershrubs, rarely shrubs or small trees, sometimes hemiparasitic or holoparasitic on roots and lacking chlorophyll
Stems
cylindrical or quadrangular, sometimes ribbed or narrowly winged
Leaves
opposite and/or alternate, or rarely whorled, sometimes fascicled or radical, simple, entire to deeply divided, rarely reduced to scales or aborted; stipules 0
Flowers
bisexual, strongly to slightly irregular, rarely subregular or regular, pedicellate or not, solitary axillary or in terminal or at times subterminal and lateral cymes or racemes, in such forms as spikes, heads, panicles or thyrses
Bracts
opposite or alternate, free or adnate to pedicel, rarely to calyx; bracteoles 0 or 2
Calyx
usually (4)5-lobed, or rarely, by modification, 2- or 3-lobed or spathaceous, usually ± united, persistent, tube from almost lacking to long, usually cylindrical to campanulate; lobes equal or not, valvate, variously overlapping or open in bud
Corolla
sympetalous, (3)4- or 5(6-8)-lobed, usually campanulate, cylindrical or ventricose or enlarged above, or bilabiate with upper (posterior) lip entire, 2- or sometimes 4-lobed, erect, concave, ± hooded, flat or spreading; lower (anterior) lip (1)3(4)-lobed, spreading; sometimes corolla ± unilabiate with tube split in front and limb of 4(5) lobes; tube straight, or variously curved to geniculate, at times oblique, sometimes with 1 or 2 spurs, sacs or hollows at base or in throat; lobes subequal or posterior pair shorter, ± spreading
Stamens
usually 4, didynamous or at times ± equal, or 2 with sometimes 2 reduced to staminodes, or 5 with fifth subrudimentary, rarely perfect, alternating with corolla lobes, exserted or included; filaments arising in corolla tube or at throat, filiform or dilated, free, confluent or decurrent down tube, occasionally with lower pair variously appendaged at base, there sometimes anterior filaments twisted around and thus occupying posterior position; anthers usually bithecate, sometimes synthecate (at length unithecate by confluence of 2 thecae), at times unithecate, free or often coherent; thecae equal or with one smaller and at times sterile; staminodes 0, 1 or 2
Nectary/disc
various, often annular or unilateral at base of ovary, sometimes obsolete
Ovary
superior, bilocular (rarely ± unilocular or trilocular), sessile, entire, with carpels median; placentas central, adnate to septum or rarely parietal; ovules usually many, sometimes few or 1 per locule, often seated on pulvinate funicle with central depression; style terminal, simple, usually filiform; stigma entire or 2(3)-lobed
Fruit
usually a capsule, loculicidal and/or septicidal, sometimes dehiscing by pores or by meridional fissures, or indehiscent and then at times separating into 2 1-seeded nutlets (cocci), or rarely 1 nutlet by abortion, seldom a berry, rarely a fleshy drupe
Seeds
small to minute, 1-many per locule, variously shaped, pitted, furrowed, ridged, ribbed or winged, rarely smooth; embryo straight to weakly curved; endosperm oily
Classification Notes:
Classification and delimitation of the
Scrophulariaceae
are problematical, and in its present circumscription the family is not considered monophyletic (Olmstead & Reeves 1995). The
Selaginaceae
, established as a family by Choisy (1823), and accepted as such by Dyer (1975), Dahlgren (1980), Cronquist (1988, under
Globulariaceae
) and Hartley & Balkwill (1990), is here included in
Scrophulariaceae
. This is in agreement with, among others, Hilliard (1990, 1994 and 1999), Philcox (1990), Brummitt (1992), Mielcarek (1996) and Takhtajan (1997)
*
Orobanchaceae
is also difficult to separate from
Scrophulariaceae
. Some genera have been moved back and forth between them, such as
Buchnera
L.,
Harveya
Hook.,
Hyobanche
L. and *
Orobanche
L. The two families have been treated as distinct by, for example, Cronquist (1988), Kreutz (1995) and Mabberley (1997). Others recognise *
Orobanchaceae
as part of
Scrophulariaceae
, such as Brummitt (1992), Thorne (1992), Mielcarek (1996) and Takhtajan (1997), and they are followed here.
Recent research is leading to publication of other classification schemes. For instance, based on evidence from morphology, DNA base-pair sequences and chemistry, Judd et al. (1999) divide the genera here placed under Scrophulariaceae into three families which they consider monophyletic:
1.
Scrophulariaceae
, which includes the closely related
Scrophularia
L. and *
Verbascum
L. These two genera are seen as closely linked phenetically to
Selago
L. and relatives (
Selagineae
) by the intermediate group of
Sutera
Roth and relatives (
Manuleae
)
2.
Plantaginaceae
, which comprises
Plantago
L.,
Bacopa
Aubl.,
Limnophila
R.Br., *
Linaria
Mill.,
Lindernia
All.,
Mimulus
L.,
Nemesia
Vent., *
Scoparia
L. and others
3. *
Orobanchaceae
, which includes the parasitic genera, such as *
Orobanche
L. and
Harveya
Hook.
Oftia
Adans. and
Hiernia
S.Moore, listed by Dyer (1975) under
Scrophulariaceae
, are retained under that family, the first with reservation.
Oftia
has been placed in
Verbenaceae
,
Myoporaceae
,
Scrophulariaceae
or in a separate family of its own. Takhtajan (1997) placed it in
Oftiaceae
, next to the
Scrophulariaceae
, but noted it shows similarities with
Teedia
, in the last family.
Oftia
is regarded here as an anomalous genus in
Scrophulariaceae
.
Charadrophila
Marloth, usually placed under
Gesneriaceae
(also by Dyer 1975), was transferred by Weber (1989) to
Scrophulariaceae
, mainly because of its capsular fruits. This was accepted by Brummitt (1992) and Mabberley (1997) and is followed here. In
Scrophulariaceae
the genus occupies an isolated position, possibly near
Alonsoa
Ruiz & Pav. (Weber 1989), although it has features aligning it with the
Rhinanathoideae
.
Some exotic species of genera such as *
Cymbalaria
Hill, *
Linaria
Mill.,
Mimulus
L., *
Verbascum
L. and
Veronica
L. are widely cultivated and may occur as garden escapes. Others are found as weeds, for example *
Kickxia
Dumort., *
Scoparia
L., *
Misopates
Raf. and *
Orobanche
L.
The southern Africa genera of
Scrophulariaceae
can be classified based mainly on the classification system of Takhtajan (1997) and groupings of genera into tribes by Hilliard (1994, 1999), Fischer (1992), Barringer (1993) and Steiner (1996 and pers. com. 2000). However, relationships are far from definite and several genera are of very uncertain affinity (marked by ? in the scheme)
Nomenclature:
Scrophulariaceae
Choisy: 71 (1823)
Bentham: 186 (1846)
Bentham: 913, 1126 (1876)
Wettstein: 39 (1891/1893)
Hallier: 181 (1903)
Hiern: 121 (1904)
Hiern & Stapf: 421 (1904)
Hemsley & Skan: 261 (1906)
Merxmüller & Roessler: 1 (1967a)
Merxmüller & Roessler: 1 (1967b)
Webb: 202 (1972)
Hilliard & Burtt: 155 (1977)
Visser: 82 (1981)
Sutton: 1 (1988)
Hilliard & Burtt: 179 (1989)
Hilliard: 315 (1990)
Philcox: 1 (1990)
Brummitt: 665 (1992)
Fischer: 1 (1992)
Hilliard: 1 (1994)
Mielcarek: 3 (1996)
Steiner: 63 (1996)
Mabberley: 1 (1997)
Retief & Herman: 548, 603, 617 (1997)
Takhtajan: 451 (1997)
Hilliard: 1 (1999)
Distribution & Notes:
Global
: Genera ± 290, species ± 4500 (including *Orobanchaceae, Selaginaceae & Charadrophila); cosmopolitan but especially temperate areas and tropical mountains
Southern Africa
: Genera ± 79 (80) genera, ± 760 species, widespread
References:
BARRINGER, K. 1993. Five new tribes in the
Scrophulariaceae
.
Novon
3
BENTHAM, G. 1846.
Scrophulariaceae
. In A.P. de Candolle,
Prodromus
10. Masson, Paris
BENTHAM, G. 1876.
Scrophularineae
. In G. Bentham & J.D. Hooker,
Genera plantarum
2. Lovell Reeve & Co., London
BRUMMITT, R.K. 1992.
Vascular plant families and genera
. Royal Botanic Gardens, Kew
CHOISY, J.D. 1823. Mémoire sur la famille des Sélaginées.
Mémoires de la Société de Physique et d' Histoire Naturelle de Genève
2(2)
FISCHER, E. 1992. Systematik der afrikanischen
Lindernieae
(
Scrophulariaceae
).
Tropische und subtropische Pflanzenwelt
81
HALLIER H. 1903. Über die Abgrenzung und Verwandtschaft der einzelnen Sippen bei den Scrophulariaceen.
Bulletin de l'Herbier Boissier
2, 3
HEMSLEY, W.B. & SKAN, S.A. 1906.
Scrophulariaceae
.
Flora of tropical Africa
4
HILLIARD, O.M. 1990. A brief survey of
Scrophulariaceae
-
Selagineae
.
Edinburgh Journal of Botany
47
HILLIARD, O.M. 1994.
The
Manuleae
. A tribe of
Scrophulariaceae
. Edinburgh University Press, Edinburgh
HILLIARD, O.M. 1999.
The tribe
Selagineae
(
Scrophulariaceae
)
. Royal Botanic Garden, Edinburgh
HILLIARD, O.M. & BURTT, B.L. 1977. Notes on some plants of southern Africa chiefly from Natal: VI.
Notes from the Royal Botanic Garden Edinburgh
35
HILLIARD, O.M. & BURTT, B.L. 1989 ('1988'). Notes on some plants of southern Africa chiefly from Natal: XV.
Notes from the Royal Botanic Garden Edinburgh
45
MABBERLEY, D.J. 1997.
The plant-book
, edn 2. Cambridge University Press, Cambridge
MERXMÜLLER, H. & ROESSLER, H. 1967a.
Scrophulariaceae
.
Prodromus einer Flora von Südwestafrika
126
MERXMÜLLER, H. & ROESSLER, H. 1967b.
Selaginaceae
.
Prodromus einer Flora von Südwestafrika
127
MIELCAREK, R. 1996. Les
Scrophulariaceae
dans la flore d'Afrique centrale (excl.
Linderneae
).
Fragmenta floristica et geobotanica
41
PHILCOX, D. 1990.
Scrophulariaceae
.
Flora zambesiaca
8,2
RETIEF, E. & HERMAN, P.P.J. 1997. Plants of the northern provinces of South Africa: keys and diagnostic characters.
Strelitzia
6
STEINER, K.E. 1996. Chromosome numbers and relationships in tribe
Hemimerideae
(
Scrophulariaceae
).
Systematic Botany
21
SUTTON, D.A. 1988.
A revision of the tribe
Antirrhineae
. British Museum (Natural History), London
TAKHTAJAN, A. 1997.
Diversity and classification of flowering plants
. Columbia University Press, New York
VISSER, J. 1981.
Scrophulariaceae
and
Orobanchaceae
.
South African parasitic flowering plants
. Juta, Cape Town
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